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                                                                                                                                                                                                                             national recommendations. However, considering that if the
                                                                                                                                                                                                                           The use of assays other than IIF is in accordance with inter-
                                                                                                             Prolonged respiratory symptoms are described both in
                                                                                                                                                                                                                             evant ANA included in the panel of these tests may be missed [7].
                                                                                                                                                                                                                             assays. Furthermore, it has been reported that some clinically rel-
                                                                                                                                                                                                                             of the test, which is a clear limitation for the use of solid-phase
                                                                                                                                                                                                                             mated assays is restricted to the antigens incorporated in the panel
                                                                                                             Dysfunctional esophageal activity accounts for the gastro-
                                                                                                                                                                                                                             mated tests may be beneficial. The diagnostic potential of auto-
                                                                                                                                                                                                                             For laboratories with a high throughput of samples, such auto-
                                                                                                                                                                                                                             ing a mixture of various extracted antigens have been developed.
                                                                                                                                                                                                                             commercially available automated solid-phase assays incorporat-
                                                                                                                                                                                                                             inter-observer variability [6]. To overcome these disadvantages,
                                                                                                                                                                                                                             well-trained analysts, is quite time-consuming, and shows high
                                                                                                                                                                                                                             overlooked by IIF [5]. Furthermore, IIF requires experienced and
                                                                                                                                                                                                                             ANA, especially anti-SSA/Ro and anti-Jo-1 antibodies, may be
                                                                                                                                                                                                                             routine [1]. However, it has been shown that some subtypes of
                                                                                                             TEF is a congenital malformation that requires early inter-
                                                                                                                                                                                                                             reference screening method for ANA in the clinical laboratory
                                                                                                                                                                                                                             ing and has been defined as the
                                                                                                                                                                                                                             the gold standard for ANA screen-
                                                                                                                                                                                                                             (IIF) on Hep-2 cells is regarded as
                                                                                                                                                                                                                           Indirect immunofluorescence
                                                                                                                                                                                                                             approach [2,4].
                                                                                                                                                                                                                             disease with an “intent to prevent”
                                                                                                                                                                                                                             medicine [3], especially for the identification of pre- or early
                                                                                                                                                                                                                             sion whether ANA represent useful biomarkers in preventive
                                                                                                                                                                                                                             sification criteria [1,2]. Beyond that, there is an open discus-
                                                                                                                                                                                                                             and polymyositis. ANA are thus incorporated in several clas-
                                                                                                             The patients with recurrence of TEF had significantly more
                                                                                                                                                                                                                             Sjögren’s syndrome, mixed connective tissue disease (MCTD),
                                                                                                                                                                                                                             systemic lupus erythematosus (SLE), systemic sclerosis (SSc),
                                                                                                                                                                                                                             T in the diagnosis of systemic autoimmune disorders such as
                                                                                                                                                                                                                           he detection of antinuclear antibodies (ANA) is important

                                                                                                             During the hospitalizations for clinical bronchiolitis, six
                                                                                                                                                                                                                              solid-phase assay
                                                                                                                                                                                                                              antinuclear antibodies (ANA), Elia CTD Screen (ECS),
                                                                                                                                                                                                                                        KEY WORDS:
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - B | 18-11-13 | 11:24:13 | SR:-- | Cyan
                                                                                                                                                                                                                                                        #131118-COHANIM - 131118-COHANIM | 4 - B | 18-11-13 | 11:24:13 | SR:-- | Black
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - B | 18-11-13 | 11:24:13 | SR:-- | Yellow
                                                                                                             The details of patients who were hospitalized for respiratory
                                                                                                                                                                                                                                                        131118-COHANIM - 131118-COHANIM | 4 - B | 18-11-13 | 11:24:13 | SR:-- | Magenta
            0.009
                   1 (1–2)
            0.42
                   9/24
            < 0.0001
                   3 (2–6)
                                                                                                                                                                                                                        1,4   Omid Amouzadeh-Ghadikolai MD , Mariana Stettin MD  and Gerhard Reicht MD
                   7/7
            0.073
            0.011
                   3 (2–6)
                                                                                                             All the patients with recurrence of TEF who were hospital-
                   34
            value
                   (n=7)
            P
                   of TEF
                                                                                                             Seven out of nine patients with recurrence of TEF and 32 of
                                                                                                                                                                                                                                                        #
       Original articles   0 (0–1)  15/30  1 (1–2)  19/32  1.5 (1–2)  57  (n=32)  of TEF   recurrence  Recurrence   No   Original articles  This study is the first to evaluate the possible association   The recurrence is usually located in the pouch of the origi-  Recurrence of TEF manifests with respiratory and gastrointes-  Pulmonary function tests demonstrate restrictive patterns in   Number of positive PCR per patient (median 25–75%)  Episodes of positive PCR during c
                   hospital electronic database. The discharge recommendations   STATISTICAl AnAlySIS                            prevalence was significantly higher in CD patients than in UC   quency among Caucasian CD patients ranges from 3–16%
                   were based on the clinical judgment of physicians during hos-  Statistical analyses were performed using IBM Statistical   patients. The mutation was observed in 8/25 (32%) of the CD   for the different NOD2/CARD15 mutations and 2–6% in UC
                   pitalization.                                   Package for the Social Sciences statistics software, version 19   patients and in 3/25 (12%) of UC patients.   patients [11-14].
                     Pre-hospitalization hemoglobin A1C (HbA1c) levels and   (SPSS, IBM Corp, Armonk, NY, USA). Categorical variables are                                          There are limited reports from the Arab world regarding
                   first month post-discharge data regarding prescription and   reported as frequency and percentages, and continuous vari-  gEnOTypE-pHEnOTypE AnAlySIS In CD pATIEnTS   NOD2/CARD15 mutations. There are several reports in differ-
                   purchasing of insulin were retrieved from the Israeli national   ables are reported as mean ± standard deviation. Categorical   Demographic and clinical data comparing the group of CD   ent Arab populations in North Africa, Tunisia, Algeria, and
                   patient database, as this information is not available in the   variables were compared using chi-square test or Fisher’s exact   mutation carriers with the non-carriers are shown in Table 2.  Morocco as well as in the Arab population in another region
                   hospital electronic database. The last available HbA1c of   test and continuous variables by independent samples t-test or   The Gly908Arg mutation carriers were younger in age
                   each patient before admission was analyzed. The results were   analysis of variance (ANOVA) test. A two-tailed P < 0.05 was   (31.38 ± 8.5 years vs. 38.88 ± 10.4 years; P = 0.07). The age at   Table 2. Demographic, clinical characteristics and genotype-phenotype correlation in
                   from 3–6 months before admission. Our study was approved   considered statistically significant. A logistic regression was   diagnosis was significantly lower among mutation carriers: 22.8   Crohn’s disease patients
                   by the research ethics committee at Assaf Harofeh Medical   done to calculate adjusted odds ratio of variables.  ± 4.5 years and 28.82 ± 9.1 years for non-carrier (P = 0.04). It         Gly908Arg carrier   Non-carrier   P
                   Center.                                                                                                       is noteworthy to mention that all mutation carriers were male   Characteristic  n=8 (32%)  n=17 (68%)  value
                                                                                                                                 (100%), whereas in the non-carrier group only 41.2% were male   Age, years, mean ± SD   31.38 ± 8.5  38.88 ± 10.4  0.07
                   pATIEnT ADHEREnCE                               RESULTS                                                       (P = 0.005). When analyzing the disease location according to   Age at diagnosis, years, mean ± SD  22.8 ± 4.5  28.82 ± 9.1  0.04
                   Adherence by patients was defined as “full adherence” if the   pATIEnT ADHEREnCE wITH DISCHARgE RECOMMEnDATIOn  the Montreal classification, no association was found between   Gender, male (%)  8 (100)  7 (41.2)  0.005
                   patient had purchased basal (long-acting) as well as bolus   The study comprised 153 patients. Of these, 81 (53.6%) were   the mutation carriers with the non-carriers. No relationship was
                   (short-acting) insulin, “partial adherence” if the patient had   male. The average age was 67.5 ± 13.1 years. Table 1 describes   found regarding other parameters including disease behavior,   Appendectomy (%)  0   5 (33.3)  0.08
                   purchased only one kind of insulin (basal or bolus), and “no   patient adherence by demographic characteristics and clini-  appendectomy history, family history of IBD, smoking history,   Family history of IBD (%)  1 (12.5)  4 (23.5)  0.47
                   adherence” if the patient did not purchase any insulin.  cal parameters. The majority of patients, 106 (69.3%), showed   treatment with anti-tumor necrosis factor (TNF), and surgery.   Smoking history (%)  2 (25.0)  6 (35.3)  0.61
                                                                   full adherence to discharge instructions. Twenty-five patients                                                Anti-TNF treatment (%)      4 (50.0)    6 (37.5)   0.45
                   pHySICIAn ADHEREnCE                             (16.3%) showed no adherence and 22 (14.4%) showed par-        gEnOTypE-pHEnOTypE AnAlySIS In uC pATIEnTS      Surgery (%)                 3 (37.5)    7 (41.2)   0.86
                   Adherence by physicians was defined as “full adherence”   tial adherence. A significant positive association was found   We analyzed the phenotypic characteristics presented by all 25   Disease duration, median, years (IQR)  5.5 (4–11.5)  6 (5–15)  0.63
                   if the primary physician had prescribed basal and bolus   between pre-hospitalization HbA1c and patient adherence.   UC patients. Of the 25 UC patients, the Gly908Arg mutation was   Localization ileal (%)  2 (25)  7 (41)   0.43
                   insulin, “partial adherence” if only one kind of insulin had   The average pre-hospitalization HbA1c was 9.04% ± 2.04 in the   detected in three (12%). When comparing mutation carriers to   L2 (%)  1 (12.5)  1 (5.9)  0.54
                   been prescribed, and “no adherence” if no insulin had been   full-adherence group, 8.67% ± 1.70 in the partial-adherence   non-carriers with regard to age, we found that Gly908Arg carri-
                   prescribed.                                     group, and 7.51% ± 1.35 in the no-adherence group (P = 0.002).   ers are older than non-carriers (67.0 ± 24.5 years vs. 41.2 ± 12.3   L3 (%)  4 (50)  8 (47)     0.61
                                                                   In addition, there was a trend toward better adherence with   years, P = 0.006, respectively). There was a trend toward older   L4 (%)    1 (12.5)    1 (5.9)    0.54
       Table 1. Patient adherence by demographic characteristics and clinical parameters   younger age that did not reach statistical significance. No   age at diagnosis (46.7 ± 16.1 years vs. 30.7 ± 12.7 years, P = 0.06).   Non-stricturing, non-penetrating disease (%)  4 (50)  12 (71)  0.32
                                                                   association was found between any other clinical and demo-    No significant associations were found regarding other param-  Stricturing-disease (%)  2 (25)  4 (24)  0.65
                     Total   no adherence  partial adherence  full adherence  p value
                                                                   graphic parameters and patient adherence.                     eters. Demographic and clinical data comparing the mutation   Penetrating-disease (%)  2 (25)  1 (5.9)   0.23
                     n=153   n=25 (16.3%)  n=22 (14.4%)  n=106 (69.3%)  Overall, these data demonstrate that patients with higher   carriers and non-carriers are shown in Table 3.
       Age, years, mean ± SD  67.5 ± 13.06  71.04 ± 12.48  70.27 ± 12.13  66.15 ± 13.24  0.14  pre-hospitalization HbA1c were significantly more compliant                       IBD = inflammatory bowel disease, IQR = interquartile range, SD = standard deviation,
                                                                                                                                                                                 TNF = tumor necrosis factor
       gender                                                      with discharge instructions for continuous BB insulin treat-
       Male          81 (53%)  13 (16%)  8 (9.8%)  60 (74%)  0.22
       Female        72 (47%)  12 (16.6%)  14 (19.4%)  46 (63.8%)  ment.                                                         DISCUSSION                                      Table 3. Demographic, clinical characteristics and genotype-
       HbA1c, %      8.74 ± 1.97  7.51 ± 1.35  8.67 ± 1.70  9.04 ± 2.04  0.002                                                   IBD prevalence in the Bedouin Arab population is increas-  phenotype correlation in ulcerative colitis patients
       BMI, kg/m 2   30.3 ± 6.0  30.6 ± 5.5  30.4 ± 6.9  30.2 ± 6.0  0.96  pHySICIAn ADHEREnCE wITH DISCHARgE RECOMMEnDATIOnS    ing [2]. In the current study, we investigated the frequency of       Gly908Arg
       Creatinine, mg/dl  1.56 ± 1.14  1.68 ± 1.64  1.88 ± 1.09  1.46 ± 1.0  0.236  Table 2 describes physician adherence by demographic char-  NOD2/CARD15 mutations in this population and its associa-  Characteristic  carrier n=3   Non-carrier   P
                                                                                                                                                                                                       (12%)
                                                                                                                                                                                                               n=22 (88%)
                                                                                                                                                                                                                        value
       BMI = body mass index, HbA1c = hemoglobin A1C, SD = standard deviation  acteristics and clinical parameters of discharged patients.   tion with the IBD phenotype. To the best of our knowledge, no
                                                                   Physician full adherence with discharge instructions was sig-  data have been previously reported regarding these mutations   Age, years, mean ± SD   67.0 ± 24.5  41.2 ± 12.3  0.006
                                                                   nificantly higher than patient full adherence, 121 (79.1%) vs.   in the Bedouin Arab population in southern Israel.   Age at diagnosis, years, mean ± SD  46.7 ± 16.1  30.7 ± 12.7  0.06
       Table 2. Physician adherence by demographic characteristics and clinical parameters of   106 (69.3%), respectively (P = 0.0182), suggesting that 20%   As expected, and in accordance with previous findings, we   Gender, male (%)  1 (33.3)  11 (50.0)
       patients                                                                                                                                                                                                         0.53
                                                                   of physicians do not prescribe insulin according to discharge   identified a higher frequency of NOD2/CARD15 mutation in   Appendectomy (%)  0   0   –
                     Total   no adherence  partial adherence  full adherence  p value  recommendations and an additional subset of patients do   CD than UC, 32% vs.12%, respectively.   Family history of IBD (%)  0   1 (4.5)  0.88
                     n=153   n=20 (13.1%)  n=12 (7.8%)  n=121 (79.1%)  not adherent to their physician’s prescription. A significant   Interestingly, in our cohort only one of the three NOD2/
       Age, years, mean ± SD  67.5 ± 13.06  72.65 ± 11.07  70.25 ± 13.7  66.43 ± 13.16  0.108  association was found between pre-hospitalization HbA1c   CARD15 variant mutations was found: the Gly908Arg muta-  Smoking history (%)  0   5 (22.7)  0.49
       gender                                                      and physician adherence as well as a trend toward better      tion. No Arg702Trp or Leu1007fsinsC mutations were found   Anti-TNF treatment (%)  0   0   –
       Male          81 (52.9%)  10 (12.3%)  6 (7.4%)  65 (80.2%)  0.932  adherence with younger age, which did not reach statisti-  among the Bedouin Arab IBD patients. In addition, no homo-  Past surgery (%)  0   2 (10.0)  0.75
       Female        72 (47.1%)  10 (13.8%)  6 (8.3%)  56 (77.7%)
                                                                   cal significance. No association was found between any        zygotes/compound heterozygotes were observed.   Proctitis (%)         1 (33.3)  4 (18.2)  0.50
       HbA1c, %      8.74 ± 1.97  7.38 ± 1.0  9.18 ± 1.6  8.93 ± 2.04  0.003
                                                                   other clinical and demographic parameters and physician         The frequency of NOD2/CARD15 mutations is relatively   Left colitis (%)  2 (66.7)  9 (40.9)  0.41
       BMI, kg/m 2   30.3 ± 6.0  29.96 ± 3.86  28.88 ± 4.71  30.5 ± 6.41  0.657  adherence.                                      high among our population. The frequency is ethnic specific   Pancolitis (%)  0  9 (41.1)  0.24
       Creatinine, mg/dl  1.56 ± 1.14  1.86 ± 1.8  1.57 ± 1.08  1.51 ± 1.01  0.437  These data demonstrate that similarly to patient adherence,   and varies in different reports and geographic region. However,   IBD = inflammatory bowel disease, SD = standard deviation, TNF = tumor
       BMI = body mass index, HbA1c = hemoglobin A1C, SD = standard deviation  pre-hospitalization HbA1c and age affect primary physician   most reports showed a prevalence of less than 30%. The fre-  necrosis factor
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